Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 21.2F, Problem 21.1P

Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where possible.

  1. a. PhCOOCH2CH(CH3)2
  2. b. PhOCHO
  3. c. PhCH(CH3)COOCH3
  4. d. PhNHCOCH2CH(CH3)2
  5. e. CH3CONHCH2Ph
  6. f. CH3CH(OH)CH2CN
  7. g. (CH3)2CHCH2COBr
  8. h. Cl2CHCOCl
  9. i. (CH3)2CHCOOCHO

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  1

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  2

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  3

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  4

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  5

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  6

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  7

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  8

Chapter 21.2F, Problem 21.1P, Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where , example  9

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Chapter 21 Solutions

Organic Chemistry (9th Edition)

Ch. 21.7C - Prob. 21.20PCh. 21.7C - Prob. 21.21PCh. 21.7D - Prob. 21.22PCh. 21.7D - The mechanism for acidic hydrolysis of a nitrile...Ch. 21.8A - Prob. 21.24PCh. 21.8C - Prob. 21.25PCh. 21.9 - Prob. 21.26PCh. 21.9 - Prob. 21.27PCh. 21.9 - Prob. 21.28PCh. 21.10 - Draw a mechanism for the acylation of anisole by...Ch. 21.10 - Prob. 21.30PCh. 21.11 - Prob. 21.31PCh. 21.11 - Prob. 21.32PCh. 21.12 - Problem 21-33 Propose a mechanism for the...Ch. 21.12 - Suggest the most appropriate reagent for each...Ch. 21.12 - Show how you would synthesize each compound,...Ch. 21.13 - Prob. 21.36PCh. 21.13 - Prob. 21.37PCh. 21.14 - Prob. 21.38PCh. 21.14 - Prob. 21.39PCh. 21.16 - Prob. 21.40PCh. 21.16 - Prob. 21.41PCh. 21 - Prob. 21.42SPCh. 21 - Give appropriate names for the following...Ch. 21 - Predict the major products formed when benzoyl...Ch. 21 - Predict the products of the following reactions....Ch. 21 - Prob. 21.46SPCh. 21 - Prob. 21.47SPCh. 21 - Prob. 21.48SPCh. 21 - Propose mechanisms for the following reactions.Ch. 21 - Prob. 21.51SPCh. 21 - An ether extraction of nutmeg gives large...Ch. 21 - Prob. 21.53SPCh. 21 - Show how you would accomplish the following...Ch. 21 - Prob. 21.55SPCh. 21 - Prob. 21.56SPCh. 21 - Prob. 21.57SPCh. 21 - Prob. 21.58SPCh. 21 - Prob. 21.59SPCh. 21 - Explain this curious result. What does this...Ch. 21 - Prob. 21.61SPCh. 21 - Prob. 21.62SPCh. 21 - Prob. 21.63SPCh. 21 - A chemist was called to an abandoned aspirin...Ch. 21 - Prob. 21.67SPCh. 21 - The IR spectrum, 13ONTVTR spectrum, and 1HNMR...Ch. 21 - Prob. 21.69SPCh. 21 - Prob. 21.70SPCh. 21 - Prob. 21.71SP
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